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Evolutionary Conservation of Infection-Induced Cell Death Inhibition among Chlamydiales

Control of host cell death is of paramount importance for the survival and replication of obligate intracellular bacteria. Among these, human pathogenic Chlamydia induces the inhibition of apoptosis in a variety of different host cells by directly interfering with cell death signaling. However, the...

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Detalles Bibliográficos
Autores principales: Karunakaran, Karthika, Mehlitz, Adrian, Rudel, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142178/
https://www.ncbi.nlm.nih.gov/pubmed/21799887
http://dx.doi.org/10.1371/journal.pone.0022528
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author Karunakaran, Karthika
Mehlitz, Adrian
Rudel, Thomas
author_facet Karunakaran, Karthika
Mehlitz, Adrian
Rudel, Thomas
author_sort Karunakaran, Karthika
collection PubMed
description Control of host cell death is of paramount importance for the survival and replication of obligate intracellular bacteria. Among these, human pathogenic Chlamydia induces the inhibition of apoptosis in a variety of different host cells by directly interfering with cell death signaling. However, the evolutionary conservation of cell death regulation has not been investigated in the order Chlamydiales, which also includes Chlamydia-like organisms with a broader host spectrum. Here, we investigated the apoptotic response of human cells infected with the Chlamydia-like organism Simkania negevensis (Sn). Simkania infected cells exhibited strong resistance to apoptosis induced by intrinsic stress or by the activation of cell death receptors. Apoptotic signaling was blocked upstream of mitochondria since Bax translocation, Bax and Bak oligomerisation and cytochrome c release were absent in these cells. Infected cells turned on pro-survival pathways like cellular Inhibitor of Apoptosis Protein 2 (cIAP-2) and the Akt/PI3K pathway. Blocking any of these inhibitory pathways sensitized infected host cell towards apoptosis induction, demonstrating their role in infection-induced apoptosis resistance. Our data support the hypothesis of evolutionary conserved signaling pathways to apoptosis resistance as common denominators in the order Chlamydiales.
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spelling pubmed-31421782011-07-28 Evolutionary Conservation of Infection-Induced Cell Death Inhibition among Chlamydiales Karunakaran, Karthika Mehlitz, Adrian Rudel, Thomas PLoS One Research Article Control of host cell death is of paramount importance for the survival and replication of obligate intracellular bacteria. Among these, human pathogenic Chlamydia induces the inhibition of apoptosis in a variety of different host cells by directly interfering with cell death signaling. However, the evolutionary conservation of cell death regulation has not been investigated in the order Chlamydiales, which also includes Chlamydia-like organisms with a broader host spectrum. Here, we investigated the apoptotic response of human cells infected with the Chlamydia-like organism Simkania negevensis (Sn). Simkania infected cells exhibited strong resistance to apoptosis induced by intrinsic stress or by the activation of cell death receptors. Apoptotic signaling was blocked upstream of mitochondria since Bax translocation, Bax and Bak oligomerisation and cytochrome c release were absent in these cells. Infected cells turned on pro-survival pathways like cellular Inhibitor of Apoptosis Protein 2 (cIAP-2) and the Akt/PI3K pathway. Blocking any of these inhibitory pathways sensitized infected host cell towards apoptosis induction, demonstrating their role in infection-induced apoptosis resistance. Our data support the hypothesis of evolutionary conserved signaling pathways to apoptosis resistance as common denominators in the order Chlamydiales. Public Library of Science 2011-07-22 /pmc/articles/PMC3142178/ /pubmed/21799887 http://dx.doi.org/10.1371/journal.pone.0022528 Text en Karunakaran et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Karunakaran, Karthika
Mehlitz, Adrian
Rudel, Thomas
Evolutionary Conservation of Infection-Induced Cell Death Inhibition among Chlamydiales
title Evolutionary Conservation of Infection-Induced Cell Death Inhibition among Chlamydiales
title_full Evolutionary Conservation of Infection-Induced Cell Death Inhibition among Chlamydiales
title_fullStr Evolutionary Conservation of Infection-Induced Cell Death Inhibition among Chlamydiales
title_full_unstemmed Evolutionary Conservation of Infection-Induced Cell Death Inhibition among Chlamydiales
title_short Evolutionary Conservation of Infection-Induced Cell Death Inhibition among Chlamydiales
title_sort evolutionary conservation of infection-induced cell death inhibition among chlamydiales
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142178/
https://www.ncbi.nlm.nih.gov/pubmed/21799887
http://dx.doi.org/10.1371/journal.pone.0022528
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